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Links from PubChem BioAssay

Items: 1 to 20 of 973

8.

BindingDB_Patents: Inhibition Assay. EGFR inhibitory activity of compounds of the present invention is quantified employing the EGFR HTRF assay.

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
AID:
1257481
9.

Inhibition of EGFR (unknown origin) after 120 mins by HotSpot assay

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
AID:
1256452
10.

Binding affinity to EGFR T790M/L858R double mutant (unknown origin)

Source:
ChEMBL
Protein Targets:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1; ...
Total:
4
11.

Binding affinity to wild type EGFR (unknown origin)

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
12.

Competitive binding affinity to human EGFR T790M mutant in presence of immobilized ligand

Source:
ChEMBL
Protein Targets:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1; ...
Total:
4
AID:
1255234
13.

Competitive binding affinity to human wild type EGFR in presence of immobilized ligand

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
14.

Inhibition of wild type EGFR phosphorylation in human A431 cells after 60 mins by mesoscale multiplex assay

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
15.

Inhibition of human EGFR after 1 hr using [gamma-32P]ATP

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
16.

Inhibition of EGFR (unknown origin) at 10 uM after 120 mins P33 radiolabeled kinase activity assay

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
17.

Inhibition of EGFR L858R mutant (unknown origin) assessed as remaining activity at 10 uM by high-throughput assay relative to control

Source:
ChEMBL
Protein Targets:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1; ...
Total:
4
18.

Inhibition of EGFR (unknown origin) assessed as remaining activity at 10 uM by high-throughput assay relative to control

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
19.

Inhibition of EGFR (unknown origin) at 1 uM by FRET method

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
20.

Inhibition of human EGFR incubated for 2 hrs by Kinase-Glo luminescent kinase assay

Source:
ChEMBL
Protein Target:
Epidermal growth factor receptor; Proto-oncogene c-ErbB-1; Receptor tyrosine-protein kinase erbB-1
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